Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517581Generated: November 3, 2026

Ethanol → 2-(2-Bromopyridin-3-yl)acetonitrile

https://huagongshe.com/reaction/1517581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantSodium CyanideHCID 8929—
Reactant2-Bromo-3-(bromomethyl)pyridineHCID 10901078—
SolventDichloromethaneHCID 6344—
Product2-(2-Bromopyridin-3-yl)acetonitrileHCID 5340350983%

Reaction Steps

A mixture of 2-bromo-3-bromomethyl-pyridine (840 mg, 3.35 mmol) and sodium cyanide (187.99 mg, 3.68 mmol) is stirred and refluxed for 1 h in a mixture water (10 mL)-ethanol (2 mL). The reaction mixture is diluted with dichloromethane and washed with saturated aqueous solution of sodium bicarbonate. The organic layer is separated, dried over magnesium sulfate and the solvent evaporated in vacuo to give 83% of the title compound that is used without further purification. MS (m/z): 197 (M+1), 199 (M+3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232289B2
Source datasetuspto-grants-2012_07
ORD IDord-259963ad65984f20a3e2916a844a5af0
Source noteuspto-grants-2012_07